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Nucleos(t)ide Analogue Treatment for Patients With Hepatitis B Virus (HBV) e Antigen-Positive Chronic HBV Genotype C Infection: A Nationwide, Multicenter, Retrospective Study

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dc.contributor.author안상훈-
dc.contributor.author이혜원-
dc.date.accessioned2023-08-09T02:43:18Z-
dc.date.available2023-08-09T02:43:18Z-
dc.date.issued2017-12-
dc.identifier.issn0022-1899-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/195777-
dc.description.abstractBackground: Antiviral treatment for hepatitis B virus (HBV) e antigen (HBeAg)-positive chronic HBV infection is still controversial. We assessed whether antiviral treatment reduces the risk of liver disease progression in these patients. Methods: This study included consecutive patients in 8 large-volume hospitals in Korea who tested positive for HBeAg and had an HBV DNA level of >20000 IU/mL, an alanine aminotransferase (ALT) level of <40 IU/L, and no evidence of cirrhosis. The primary end point was the development of hepatocellular carcinoma (HCC), and the secondary end point was the development of cirrhosis. Results: A total of 484 patients were included: 87 were in the antiviral treatment group, and 397 were in the control group. Baseline liver function was significantly more favorable for the control group. After matching for propensity score to overcome those differences, the antiviral treatment group had a significantly reduced risk for HCC (hazard ratio [HR], 0.234; log-rank P = .046) and cirrhosis (HR, 0.235; log-rank P = .015), compared with the control group. After balancing the baseline characteristics by using inverse probability weighting, antiviral therapy significantly decreased the risk of HCC (HR, 0.189; log-rank P = .004) and cirrhosis (HR, 0.347; log-rank P = .036). Conclusion: Antiviral therapy for patients with HBeAg-positive chronic HBV infection and have a high HBV load reduces the risk of HCC, even if the ALT level is below the upper limit of normal.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherOxford University Press-
dc.relation.isPartOfJOURNAL OF INFECTIOUS DISEASES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAlanine Transaminase / blood-
dc.subject.MESHAntiviral Agents / therapeutic use*-
dc.subject.MESHCarcinoma, Hepatocellular / virology-
dc.subject.MESHDNA, Viral / blood-
dc.subject.MESHFemale-
dc.subject.MESHGenotype-
dc.subject.MESHHepatitis B e Antigens / blood-
dc.subject.MESHHepatitis B e Antigens / immunology*-
dc.subject.MESHHepatitis B virus / drug effects*-
dc.subject.MESHHepatitis B virus / pathogenicity*-
dc.subject.MESHHepatitis B, Chronic / drug therapy*-
dc.subject.MESHHumans-
dc.subject.MESHLiver Cirrhosis / virology-
dc.subject.MESHLiver Neoplasms / virology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMultivariate Analysis-
dc.subject.MESHNucleosides / therapeutic use*-
dc.subject.MESHNucleotides / therapeutic use*-
dc.subject.MESHPharmacogenomic Testing-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHRisk Factors-
dc.subject.MESHTreatment Outcome-
dc.titleNucleos(t)ide Analogue Treatment for Patients With Hepatitis B Virus (HBV) e Antigen-Positive Chronic HBV Genotype C Infection: A Nationwide, Multicenter, Retrospective Study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorYoung Chang-
dc.contributor.googleauthorWon Hyeok Choe-
dc.contributor.googleauthorDong Hyun Sinn-
dc.contributor.googleauthorJeong-Hoon Lee-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorHyewon Lee-
dc.contributor.googleauthorJae-Jun Shim-
dc.contributor.googleauthorDae Won Jun-
dc.contributor.googleauthorSoo Young Park-
dc.contributor.googleauthorJoon Yeul Nam-
dc.contributor.googleauthorEun Ju Cho-
dc.contributor.googleauthorSu Jong Yu-
dc.contributor.googleauthorDong Ho Lee-
dc.contributor.googleauthorJeong Min Lee-
dc.contributor.googleauthorYoon Jun Kim-
dc.contributor.googleauthorSo Young Kwon-
dc.contributor.googleauthorSeung Woon Paik-
dc.contributor.googleauthorJung-Hwan Yoon-
dc.identifier.doi10.1093/infdis/jix506-
dc.contributor.localIdA02226-
dc.contributor.localIdA03318-
dc.relation.journalcodeJ01454-
dc.identifier.eissn1537-6613-
dc.identifier.pmid29029102-
dc.identifier.urlhttps://academic.oup.com/jid/article/216/11/1407/4210686-
dc.subject.keywordImmune-tolerant phase-
dc.subject.keywordantiviral treatment-
dc.subject.keywordhepatocellular carcinoma-
dc.subject.keywordliver cirrhosis-
dc.contributor.alternativeNameAhn, Sang Hoon-
dc.contributor.affiliatedAuthor안상훈-
dc.contributor.affiliatedAuthor이혜원-
dc.citation.volume216-
dc.citation.number11-
dc.citation.startPage1407-
dc.citation.endPage1414-
dc.identifier.bibliographicCitationJOURNAL OF INFECTIOUS DISEASES, Vol.216(11) : 1407-1414, 2017-12-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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